Canonical Allele Identifier: CA9461346
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs764357679

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422966A>C , CM000681.2:g.41422966A>C GRCh38
NC_000019.9:g.41928871A>C , CM000681.1:g.41928871A>C GRCh37
NC_000019.8:g.46620711A>C NCBI36
NG_013004.1:g.30178A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.996-32A>C MANE Select ENSP00000269980.2:n.996-32A>C
ENST00000269980.6:c.996-32A>C ENSP00000269980.2:n.996-32A>C
ENST00000457836.6:c.973A>C ENSP00000416000.2:p.Thr325Pro
ENST00000540732.3:c.1098-32A>C ENSP00000443246.1:n.1098-32A>C
ENST00000542943.5:c.909-32A>C ENSP00000440345.1:n.909-32A>C
ENST00000595085.5:c.922+269A>C ENSP00000471150.2:n.922+269A>C
NM_000709.3:c.996-32A>C NP_000700.1:n.996-32A>C
NM_001164783.1:c.993-32A>C NP_001158255.1:n.993-32A>C
NM_000709.4:c.996-32A>C MANE Select NP_000700.1:n.996-32A>C
NM_001164783.2:c.993-32A>C NP_001158255.1:n.993-32A>C